EP4626852A1 - Multi-reactor systems and methods for propylene production - Google Patents
Multi-reactor systems and methods for propylene productionInfo
- Publication number
- EP4626852A1 EP4626852A1 EP23817821.4A EP23817821A EP4626852A1 EP 4626852 A1 EP4626852 A1 EP 4626852A1 EP 23817821 A EP23817821 A EP 23817821A EP 4626852 A1 EP4626852 A1 EP 4626852A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- stream
- propylene
- metathesis
- reactor
- hydrocarbons
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
- C07C4/02—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction
- C07C4/06—Catalytic processes
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
- C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
- C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/02—Boron or aluminium; Oxides or hydroxides thereof
- C07C2521/04—Alumina
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- C07C2521/08—Silica
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/24—Chromium, molybdenum or tungsten
- C07C2523/30—Tungsten
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/32—Manganese, technetium or rhenium
- C07C2523/36—Rhenium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/40—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11
Definitions
- the present disclosure generally relates to systems and methods for producing propylene from C4 hydrocarbon streams. More specifically, the present disclosure relates to, among other embodiments, systems and methods for producing propylene through the parallel operation of separate metathesis and cracking reactors.
- Propylene is a desirable industrial compound having a worldwide production greater than that of any other organic compound other than ethylene. Accordingly, propylene is the second most important starting feedstock in the petrochemical industry after ethylene. Propylene is particularly used as a feedstock for the production of polypropylene which has a wide variety of uses. Propylene is also used for the production of isopropanol, epichlorohydrin, propylene oxide, acrylonitrile, cumene, butyraldehyde, and acrylic acid, among other important chemicals. Over 85 million tons of propylene are produced worldwide each year. In addition to other production methods, propylene may be generated by the steam cracking of hydrocarbons. Accordingly, methods and systems capable of efficient propylene production from hydrocarbon feedstocks and improving feedstock utilization of hydrocarbon streams are desirable.
- Applicants have developed systems and methods for producing propylene from hydrocarbon streams through parallel operation of separate metathesis and cracking reactors.
- the presently disclosed systems and methods may be particularly suited, to produce propylene from low cost C4 raffinate streams, that may include 1 -butene, trans-2-butene, cis-2-butene, and mixtures thereof, thereby converting low value butene streams to high value propylene.
- the operation of separate reactors provides for, among other advantages, the use of a metathesis catalyst and a cracking catalyst under separate operating conditions, thereby maximizing propylene yield. Additionally, among other advantages, the use of a separate metathesis reactor allows for the use of low temperatures metathesis catalysts in certain embodiments and high temperature metathesis catalysts in certain other embodiments.
- the method for production of propylene may include supplying a C4 raffinate hydrocarbon stream to a metathesis reactor to produce a metathesis outlet stream.
- the C4 raffinate hydrocarbon stream may substantially contain one or more C4 hydrocarbons and the metathesis outlet stream may contain a plurality of C5+ hydrocarbons, propylene, and one or more C4 hydrocarbons.
- the method may further include separating the plurality of C5+ hydrocarbons from the propylene and the one or more C4 hydrocarbons in the metathesis outlet stream to produce a C5+ feed stream and a first propylene-rich stream.
- the method may further include supplying the C4 raffinate hydrocarbon stream to an isomerization reactor prior to supplying the C4 raffinate hydrocarbon stream to the metathesis reactor.
- the C4 raffinate hydrocarbon stream may include a portion of the metathesis outlet stream and a portion of the cracked outlet stream.
- the C4 raffinate hydrocarbon stream may include an input C4 raffinate hydrocarbon stream from a source other than the outlet streams of the metathesis reactor, the cracking reactor, and the isomerization reactor.
- the method may further include supplying the metathesis outlet stream to a sequence of separation columns to produce the C5+ feed stream and the first propylene-rich stream.
- a system for the production of propylene may include a metathesis reactor operable to receive a C4 raffinate hydrocarbon stream and produce a metathesis outlet stream.
- the C4 raffinate hydrocarbon stream may substantially contain one or more C4 hydrocarbons and the metathesis outlet stream may contain a plurality of C5+ hydrocarbons, propylene, and one or more C4 hydrocarbons.
- the system may also contain a plurality of separation columns in fluid communication with the metathesis reactor and the cracking reactor. The plurality of separation columns may be operable to receive the metathesis outlet stream and produce a C5+ feed stream and a first propylene-rich stream.
- the system may also contain a cracking reactor in fluid communication with the plurality of separation columns and operable to receive the C5+ feed stream and produce a cracked outlet stream containing propylene and the one or more C4 hydrocarbons.
- the cracked outlet stream may be supplied to the plurality of separation columns whereby the propylene is separated from the one or more C4 hydrocarbons in the cracked outlet stream to produce a second propylene-rich stream and a C4-rich stream.
- the C4-rich stream may be recycled to the metathesis reactor as part of the C4 raffinate hydrocarbon stream.
- the plurality of separation columns may be further operable to separate propylene from the cracked outlet stream.
- the plurality of separation columns may include, for example, a deethanizer column, a depropanizer column, and a debutanizer column.
- the system may further include an isomerization reactor in fluid communication with the metathesis reactor and the plurality of separation columns. In such embodiments, the isomerization reactor may be operable to pretreat the C4 raffinate hydrocarbon stream prior to supplying the C4 raffinate hydrocarbon stream to the metathesis reactor.
- the system may include an isomerization reactor in fluid communication with the metathesis reactor and the plurality of separation columns.
- the isomerization reactor may be operable to receive one of an input C4 raffinate hydrocarbon stream or a combined C4 raffinate hydrocarbon stream formed from the combination of an input C4 raffinate hydrocarbon stream and the C4-rich stream or a portion of the cracked outlet stream containing C4 hydrocarbons.
- the isomerization reactor may be configured to produce an isomerized C4 raffinate hydrocarbon stream for supplying to the metathesis reactor.
- the metathesis reactor and the cracking reactor may be operated at different temperatures.
- the metathesis reactor may be a high temperature metathesis reactor that includes a tungstate on silica catalyst and that is operated at a temperature from about 500°C to about 550°C.
- the metathesis reactor may be a low temperature metathesis reactor that includes a rhenium on alumina catalyst and that is operated at a temperature from about 50°C to about 100°C.
- the cracking reactor includes a high silica ZSM-5 catalyst and is operated at a temperature from about 550°C to about 575°C.
- the system may be operable to produce a propylene product distribution in excess of 40 mol% when the C4 raffinate hydrocarbon stream contains about 70 mol% cis-2-butene and trans-2-butene and about 30 mol% n- butane.
- FIG. 1 is a graphical representation of a system and method for producing propylene from a C4 raffinate hydrocarbon feed stream, according to an exemplary embodiment of the present disclosure.
- FIG. 2 is a graphical representation of the simulated product yield distribution obtained using the system and method depicted in FIG. 1 , according to an exemplary embodiment of the present disclosure.
- the term “rich” with respect to a component X in a stream refers to component X being present in an amount greater than 50 weight percent of the totality of all components in the stream.
- a propylene-rich stream contains propylene in an amount greater than 50 weight percent of the totality of all components in the stream.
- the term “substantially” with respect to a component X in a stream, when used in the claims and/or the specification, refers to component X being present in an amount greater than 90 weight percent of the totality of all components in the stream.
- the presently disclosed systems and methods may be particularly suited, to produce propylene from low cost C4 raffinate streams, that may include 1 -butene, trans-2-butene, cis-2-butene, and mixtures thereof, thereby converting low value butene streams to high value propylene.
- the presently disclosed systems and methods include parallel operation of separate metathesis and cracking reactors which provides for, among other advantages, the use of a metathesis catalyst and a cracking catalyst under separate operating conditions, thereby maximizing propylene yield.
- an advantage of the presently disclosed methods and systems having separate metathesis and cracking reactors is that the outlet stream of the metathesis reactor may be fed to one or more separator units prior to feeding the stream to cracking reactor, thereby enhancing the cracking efficiency and providing an overall yield approaching 99%.
- systems and methods that carry out metathesis and cracking in a single unit, such as a dual bed reactor provides only approximately a 96% yield.
- the overall yield of propylene is compensated with little formation of propane in the final product slate, thereby decreasing the propylene yield by approximately 3%.
- Decoupling the metathesis and cracking reactors offers the advantage of operating the metathesis catalysts and the cracking catalysts at their optimal temperatures to maximize yield as well as lifetimes. It also allows provides the option to optimize recycle streams and operate the reactors at the higher conversion possible.
- the cracking reactor is configured to only process C5+ hydrocarbons, particularly the C5+ heavy hydrocarbons produced from the metathesis reaction.
- the metathesis reactor is configured to only process C4 hydrocarbon feed streams.
- the isomerization reactor is operable to isomerize the C4 raffinate feed stream and any other C4 recycle stream 414 in the form of C4 raffinate pretreatment stream 401 to produce isomerized C4 stream 402 by converting butenes to equilibrium.
- Isomerized C4 stream 402 may be optionally supplied to a metathesis preheater 212 to produce a preheated C4 stream 403.
- Preheated C4 stream 403 may then be supplied to metathesis heater 214 to generate a heated C4 stream 404 or metathesis reactor inlet stream 404.
- Heated C4 stream/metathesis reactor inlet stream 404 may then be fed to metathesis reactor 220 to generate metathesis reactor outlet stream 405.
- Metathesis reactor outlet stream 405 may be optionally fed to preheater 212 before being fed to a plurality of separation columns 240, 250, 260.
- metathesis reactor outlet stream 405 may be supplied to preheater 212 to form deethanizer feed from metathesis reactor stream 406.
- Deethanizer feed from metathesis reactor stream 406 may be combined with deethanizer feed from cracking reactor stream 420 to form deethanizer column feed stream 407 which may in turn be supplied to deethanizer column 240.
- Deethanizer column 240 is operable to receive the deethanizer column feed stream 407 and generate ethylene 409 in addition to light gas purge 408 and deethanizer outlet stream/depropanizer column feed 410.
- Cracking reactor preheater 222 is operable to preheat C5+ recycle stream 416 to produce preheated C5+ recycle stream 417.
- Preheated C5+ recycle stream 417 may be supplied to cracking reactor heater 224 to produce heated C5+ recycle stream/cracking reactor inlet stream 418.
- Cracking reactor inlet stream 418 may be supplied to cracking reactor 230 to generate cracking reactor outlet stream 419.
- Cracking reactor outlet stream 419 may be preheated at cracking reactor preheater 222 to generate deethanizer feed from cracking reactor stream 420, which may in turn be combined with deethanizer feed from metathesis reactor stream 406 to form deethanizer column feed stream 407 for supply to dethanizer column 240.
- method 100 may include supplying a C4 raffinate hydrocarbon stream 400, 401, 404 to a metathesis reactor 220 to produce a metathesis outlet stream 405.
- the C4 raffinate hydrocarbon stream 400, 401 may substantially contain one or more C4 hydrocarbons and the metathesis outlet stream 405 may containing a plurality of C5+ hydrocarbons, propylene, and one or more C4 hydrocarbons.
- system 200 may include a metathesis reactor 220 operable to receive a C4 raffinate hydrocarbon stream 400, 401 and produce a metathesis outlet stream 405.
- the C4 raffinate hydrocarbon stream 400, 401 may substantially contain one or more C4 hydrocarbons and the metathesis outlet stream 405 may contain a plurality of C5+ hydrocarbons, propylene, and one or more C4 hydrocarbons.
- System 200 may also include a plurality of separation columns, such as separation columns 240, 250, 260 in fluid communication with the metathesis reactor 220 and the cracking reactor 230.
- System 200 may further include an isomerization reactor 210 in fluid communication with the metathesis reactor 220 and the plurality of separation columns 240, 250, 260.
- the isomerization reactor may be operable to pretreat the C4 raffinate hydrocarbon stream 400, 401 prior to supplying the C4 raffinate hydrocarbon stream 404 to the metathesis reactor 220.
- the isomerization reactor 210 may be operable to receive one of an input C4 raffinate hydrocarbon stream 400 or a combined C4 raffinate hydrocarbon stream 401 formed from the combination of an input C4 raffinate hydrocarbon stream 400 and the C4-rich stream 414 and/or a portion of the cracked outlet stream containing C4 hydrocarbons 419, 414.
- the isomerization reactor 210 may also be configured to produce an isomerized C4 raffinate hydrocarbon stream 402 for supplying to the metathesis reactor 220.
- the metathesis reactor 220 and the cracking reactor 230 may be fixed bed reactors. In certain embodiments, the metathesis reactor 220 and the cracking reactor 230 may be operated at different temperatures.
- the metathesis reactor 220 may be a high temperature metathesis reactor 220 that includes a tungstate on silica catalyst and that is operated at a temperature from about 500°C to about 550°C.
- the metathesis reactor 220 may be a low temperature metathesis reactor 220 that includes a rhenium on alumina catalyst and that is operated at a temperature from about 50°C to about 100°C.
- the cracking reactor 230 includes a high silica ZSM-5 catalyst and is operated at a temperature from about 550°C to about 575°C.
- the system 200 may be operable to produce a propylene product distribution in excess of 40 mol% when the C4 raffinate hydrocarbon stream contains about 70 mol% cis-2-butene and trans-2-butene and about 30 mol% n-butane.
- Production yields for method 100 and system 200 depicted in FIG. 1 are shown in Table 1 as determined by simulation using an AspenPluslO simulator based on the use of a W/Si catalyst and a C4 raffinate feed stream containing a mixture of 30 mol% n-butane and 70 mol% cis-2- butene and trans-2-butene.
- the simulated product yield distributions are provided in Tables 1 and
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP22210382 | 2022-11-29 | ||
| PCT/IB2023/061986 WO2024116073A1 (en) | 2022-11-29 | 2023-11-28 | Multi-reactor systems and methods for propylene production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP4626852A1 true EP4626852A1 (en) | 2025-10-08 |
Family
ID=89076079
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP23817821.4A Pending EP4626852A1 (en) | 2022-11-29 | 2023-11-28 | Multi-reactor systems and methods for propylene production |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP4626852A1 (en) |
| CN (1) | CN120282941A (en) |
| WO (1) | WO2024116073A1 (en) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10059645B2 (en) * | 2015-07-02 | 2018-08-28 | Saudi Arabian Oil Company | Systems and methods for producing propylene |
| US11572516B2 (en) * | 2020-03-26 | 2023-02-07 | Saudi Arabian Oil Company | Systems and processes integrating steam cracking with dual catalyst metathesis for producing olefins |
-
2023
- 2023-11-28 CN CN202380081940.5A patent/CN120282941A/en active Pending
- 2023-11-28 WO PCT/IB2023/061986 patent/WO2024116073A1/en not_active Ceased
- 2023-11-28 EP EP23817821.4A patent/EP4626852A1/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CN120282941A (en) | 2025-07-08 |
| WO2024116073A1 (en) | 2024-06-06 |
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